BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

198 related articles for article (PubMed ID: 24440239)

  • 1. Spectrum and distribution of CFTR gene mutations in asthma and chronic pancreatitis cases of North Indian population.
    Muthuswamy S; Agarwal S; Awasthi S; Singh S; Dixit P; Maurya N; Choudhuri G
    Gene; 2014 Apr; 539(1):125-31. PubMed ID: 24440239
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Frequency of CFTR, SPINK1, and cathepsin B gene mutation in North Indian population: connections between genetics and clinical data.
    Singh S; Choudhuri G; Agarwal S
    ScientificWorldJournal; 2014; 2014():763195. PubMed ID: 24616641
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association of CFTR gene mutation with bronchial asthma and its severity in Indian children: a case-control study.
    Awasthi S; Maurya N; Agarwal S; Dixit P; Muthuswamy S; Singh S
    Ann Hum Biol; 2012 Mar; 39(2):113-21. PubMed ID: 22324837
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Independent contribution of common CFTR variants to chronic pancreatitis.
    de Cid R; Ramos MD; Aparisi L; García C; Mora J; Estivill X; Farré A; Casals T
    Pancreas; 2010 Mar; 39(2):209-15. PubMed ID: 19812525
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterisation of mutations and genotype-phenotype correlation in cystic fibrosis: experience from India.
    Shastri SS; Kabra M; Kabra SK; Pandey RM; Menon PS
    J Cyst Fibros; 2008 Mar; 7(2):110-5. PubMed ID: 17716958
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?
    Scotet V; Audrézet MP; Roussey M; Rault G; Dirou-Prigent A; Journel H; Moisan-Petit V; Storni V; Férec C
    Pediatrics; 2006 Nov; 118(5):e1523-9. PubMed ID: 17015492
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screening.
    Thauvin-Robinet C; Munck A; Huet F; Génin E; Bellis G; Gautier E; Audrézet MP; Férec C; Lalau G; Georges MD; Claustres M; Bienvenu T; Gérard B; Boisseau P; Cabet-Bey F; Feldmann D; Clavel C; Bieth E; Iron A; Simon-Bouy B; Costa C; Medina R; Leclerc J; Hubert D; Nové-Josserand R; Sermet-Gaudelus I; Rault G; Flori J; Leroy S; Wizla N; Bellon G; Haloun A; Perez-Martin S; d'Acremont G; Corvol H; Clément A; Houssin E; Binquet C; Bonithon-Kopp C; Alberti-Boulmé C; Morris MA; Faivre L; Goossens M; Roussey M; ; Girodon E
    J Med Genet; 2009 Nov; 46(11):752-8. PubMed ID: 19880712
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Complete cystic fibrosis transmembrane conductance regulator gene sequencing in patients with idiopathic chronic pancreatitis and controls.
    Weiss FU; Simon P; Bogdanova N; Mayerle J; Dworniczak B; Horst J; Lerch MM
    Gut; 2005 Oct; 54(10):1456-60. PubMed ID: 15987793
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Carrier frequency of F508del mutation of cystic fibrosis in Indian population.
    Kapoor V; Shastri SS; Kabra M; Kabra SK; Ramachandran V; Arora S; Balakrishnan P; Deorari AK; Paul VK
    J Cyst Fibros; 2006 Jan; 5(1):43-6. PubMed ID: 16311077
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M
    Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical phenotype of cystic fibrosis patients with the G551D mutation.
    Comer DM; Ennis M; McDowell C; Beattie D; Rendall J; Hall V; Elborn JS
    QJM; 2009 Nov; 102(11):793-8. PubMed ID: 19734299
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R; Kianishirazi R; Cassiman JJ; Zamani M; Cuppens H
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Natural history of pancreatitis associated with cystic fibrosis gene mutations.
    Frulloni L; Castellani C; Bovo P; Vaona B; Calore B; Liani C; Mastella G; Cavallini G
    Dig Liver Dis; 2003 Mar; 35(3):179-85. PubMed ID: 12779072
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
    Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
    Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [The frequency and spectrum of mutations and the IVS8-T polymorphism of the CFTR gene in Russian infertile men].
    Chernykh VB; Stepanova AA; Beskorovaĭnaia TS; Sorokina TM; Shileĭko LV; Kurilo LF; Poliakov AV
    Genetika; 2010 Jun; 46(6):844-52. PubMed ID: 20734777
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Frequency of cystic fibrosis transmembrane conductance regulator gene mutations and 5T allele in patients with allergic bronchopulmonary aspergillosis.
    Marchand E; Verellen-Dumoulin C; Mairesse M; Delaunois L; Brancaleone P; Rahier JF; Vandenplas O
    Chest; 2001 Mar; 119(3):762-7. PubMed ID: 11243954
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A novel exon duplication of the cystic fibrosis transmembrane conductance regulator in a patient presenting with adult-onset recurrent pancreatitis.
    Kopp BT; Pastore MT; Sturm AC; Holtzlander MJ; Westman JA
    Pancreas; 2011 Jul; 40(5):773-7. PubMed ID: 21673536
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First study of CF mutations in the CFTR gene of Iranian patients: detection of DeltaF508, G542X, W1282X, A120T, R117H, and R347H mutations.
    Jalalirad M; Houshmand M; Mirfakhraie R; Goharbari MH; Mirzajani F
    J Trop Pediatr; 2004 Dec; 50(6):359-61. PubMed ID: 15537723
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cystic fibrosis transmembrane conductance regulator mutation spectrum in patients with cystic fibrosis in Tunisia.
    Fredj SH; Messaoud T; Templin C; des Georges M; Fattoum S; Claustres M
    Genet Test Mol Biomarkers; 2009 Oct; 13(5):577-81. PubMed ID: 19715466
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of the entire coding region of the cystic fibrosis transmembrane regulator gene in idiopathic pancreatitis.
    Castellani C; Gomez Lira M; Frulloni L; Delmarco A; Marzari M; Bonizzato A; Cavallini G; Pignatti P; Mastella G
    Hum Mutat; 2001 Aug; 18(2):166. PubMed ID: 11462247
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.